Modulation of Ca2+Entry by Polypeptides of the Inositol 1,4,5-Trisphosphate Receptor (IP3R) That Bind Transient Receptor Potential (TRP): Evidence for Roles of TRP and IP3R in Store Depletion-Activated Ca2+Entry

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 96; no. 26; pp. 14955 - 14960
• Main Authors: Boulay, Guylain, Brown, Darren M., Qin, Ning, Jiang, Meisheng, Dietrich, Alexander, Zhu, Michael Xi, Chen, Zhangguo, Birnbaumer, Mariel, Mikoshiba, Katsuhiko, Birnbaumer, Lutz
• Format: Journal Article
• Language: English
• Published: National Academy of Sciences of the United States of America 21.12.1999; National Acad Sciences; The National Academy of Sciences
• Subjects: Amino acids; Biochemistry; Biological Sciences; Cell membranes; Cellular immunity; Complementary DNA; Drug interactions; Epitopes; Inositol 1; Proteins; Receptors
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.96.26.14955

Homologues of Drosophilia transient receptor potential (TRP) have been proposed to be unitary subunits of plasma membrane ion channels that are activated as a consequence of active or passive depletion of Ca2+stores. In agreement with this hypothesis, cells expressing TRPs display novel Ca2+- permeable cation channels that can be activated by the inositol 1,4,5-trisphosphate receptor (IP3R) protein. Expression of TRPs alters cells in many ways, including up-regulation of IP3Rs not coded for by TRP genes, and proof that TRP forms channels of these and other cells is still missing. Here, we document physical interaction of TRP and IP3R by coimmunoprecipitation and glutathione S-transferase-pulldown experiments and identify two regions of IP3R, F2q and F2g, that interact with one region of TRP, C7. These interacting regions were expressed in cells with an unmodified complement of TRPs and IP3Rs to study their effect on agonist- as well as store depletion-induced Ca2+entry and to test for a role of their respective binding partners in Ca2+entry. C7 and an F2q-containing fragment of IP3R decreased both forms of Ca2+entry. In contrast, F2g enhanced the two forms of Ca2+entry. We conclude that store depletion-activated Ca2+entry occurs through channels that have TRPs as one of their normal structural components, and that these channels are directly activated by IP3Rs, IP3Rs, therefore, have the dual role of releasing Ca2+from stores and activating Ca2+influx in response to either increasing IP3 or decreasing lumina Ca2+.